drugset / Trial / NCT02337855
A Phase I Study of the Safety, Reactogenicity, and Immunogenicity of Sm-TSP-2/Alhydrogel® With or Without GLA-AF for Intestinal Schistosomiasis in Healthy Adults
RandomizedParallel-groupDouble-blindPrevention
Summary
This is a Phase I, first-in-human study of a vaccine against S. mansoni infection.The study will recruit 72 healthy adult males and non-pregnant females from a single clinical center to test two formulations of Sm-TSP-2 vaccine (using the Alhydrogel® only, and using Alhydrogel® plus GLA-AF), each at 3 different doses: 10ug, 30ug, and 100ug. The primary objective is to assess the safety and reactogenicity of ascending doses of Sm-TSP-2/Alhydrogel® (10ug, 30ug, or 100ug) with or without GLA-AF vaccine given as three doses administered on Days 1, 57, and 113.
Timeline
- Start
- 2015-02-04
- Primary completion
- 2017-01-27
- Completion
- 2017-01-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GLA-AF | Other / unclassified | — | Intramuscular |
| Subject | Sm-TSP-2 | Vaccine | 10 ug | Intramuscular |
| Subject | Sm-TSP-2 | Vaccine | 30 ug | Intramuscular |
| Subject | Sm-TSP-2 | Vaccine | 100 ug | Intramuscular |
| Background | Aluminum hydroxide | Unknown | — | Intramuscular |